Telmisartan and Hydrochlorothiazide
- Product NDC
- 70771-1124
- 11-digit product format
- 707711124
- Labeler code
- 70771
- Product ID
- 70771-1124_83bc89db-4caf-4b60-899e-fd45a1474650
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Telmisartan and Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA204221
- Marketing category
- ANDA
- Marketing start
- 2017-10-12
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE; TELMISARTAN
- Active strength
- 13 mg/1; mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1124-3 | 70771112403 | 30 TABLET in 1 BOTTLE (70771-1124-3) | 30 tablet | 2017-10-12 | 0000-00-00 | No | No | Current |
| 70771-1124-8 | 70771112408 | 3 BLISTER PACK in 1 CARTON (70771-1124-8) > 10 TABLET in 1 BLISTER PACK (70771-1124-2) | 3 blister pack | 2017-10-12 | 0000-00-00 | No | No | Current |
| 70771-1124-9 | 70771112409 | 90 TABLET in 1 BOTTLE (70771-1124-9) | 90 tablet | 2017-10-12 | 0000-00-00 | No | No | Current |